A STUDY TO SEE THE EFFECTS OF PLACING A MATERIAL MADE OF PATIENTS OWN BLOOD IN IMPLANT PLACED IMMEDIATELY AFTER REMOVAL OF TOOTH
- Conditions
- Health Condition 1: K083- Retained dental root
- Registration Number
- CTRI/2021/04/032917
- Lead Sponsor
- MONAL SONI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 18
1.Patient with age group between 18-65 years.
2.Patient, who are cooperative, motivated and with good oral hygiene.
3.Patients with no acute infection.
4.Patients with sufficient bone volume at the site of immediate implant placement.
5.Patients who are willing and available for recall follow ups.
6.Teeth indicated for extraction with terminal periodontal disease.
7.Teeth indicated for extraction due to causes like root fracture, grossly decayed, root resorption etc.
1.Patient unable to maintain adequate oral hygiene.
2.Patients with any known systemic disease/conditions and/or on medication known to interfere with wound healing.
3.Patients who are current smokers or consume any other form of tobacco.
4.Patients with para-functional habits & traumatic occlusion.
5.Patients with severe malocclusion or crowding.
6.Teeth with periapical pathologies.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome: evaluation will be done clinically and radiographically. <br/ ><br>1.Tissue biotype assessment <br/ ><br>2. Radiographic evaluation (standardized Periapical radiograph with grid) for peri-implant bone loss and radiolucency. <br/ ><br>Timepoint: AFTER 10 DAYS, 1 MONTH, 3 MONTHS AND 6 MONTHS <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1.Modified Plaque index <br/ ><br>2. Modified sulcus bleeding index <br/ ><br>3.Peri-implant pocket depth <br/ ><br>4.Implant stability <br/ ><br>Timepoint: AFTER 10 DAYS, 1 MONTH, 3 MONTHS AND 6 MONTHS